A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995524



Internal ID20562564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94661253..94664924hg38UCSC Ensembl
chr11:94394419..94398090hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383672
hg193672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461490
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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